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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1739783생성일: 2026년 10월 26일

Bromobenzene → (+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyI-4a-(3-methoxyphenyl)-6-phenyl-6-isoquinolinol

https://huagongshe.com/reaction/1739783

반응식

참여 물질

역할이름HCID투입량
반응물BromobenzeneHCID 7961—
반응물(+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinoneHCID 10517409—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Ammonium HydroxideHCID 14923—
생성물(+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyI-4a-(3-methoxyphenyl)-6-phenyl-6-isoquinolinolHCID 8675462552.1%

반응 조건

온도-20 °C

반응 단계

30 ml (41.7 mmol) of a 1.4 M solution of n-butyllithium in hexane were added dropwise, under a nitrogen atmosphere and at -55° C., to a solution of 6.5 g (41.7 mmol) of bromobenzene in 30 ml of dry THF. After 1 h the solution was allowed to warm up to -20° C. and a solution of 2.4 g (8.3 mmol) of (±)-trans-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinone in 20 ml of dry THF was added. The reaction mixture was allowed to warm up to room temperature overnight, then it was quenched with 30 ml of a 5% HCl solution and the phases were separated. The aqueous phase was extracted with AcOEt, then brought to pH 14 with a 2N NaOH solution and extracted with AcOEt. The organic phase was dried over Na2SO4 and the solvent was removed in vacuo. The crude reaction mixture was purified by flash chromatography, eluting with a mixture CH2Cl2 /MeOH/conc. NH4OH 90:7:0.7 respectively, yielding 0.79 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05968949
출처 데이터셋uspto-grants-1999_10
ORD IDord-2f8deed0a8bc40f196403bb5701a411d
출처 메모uspto-grants-1999_10